Adsorption of rubidium ion from aqueous solution by surface ion imprinted materials

A new type of rubidium ion-imprinted polymer has been synthesized by the surface-imprinting technique using methacrylic acid as the functional monomer,the rubidium ion as the template,methanol as the solvent,and silica as a carrier.Ethylene glycol dimethacrylate and 2,2-azobisisobutyronitrile were used as acrosslinker and an initiator,respectively.In addition,based on the macrocyclic effect of crown ethers,the 18-crown-6 ligand was introduced as a ligand to fix the template ions better.Scanning electron microscopy,zeta-potential analysis,Fourier transform infrared spectroscopy,thermogravimetric analysis,and X-ray photoelectron spectroscopy were performed to characterize the ion-imprinted polymer.The effects of the preparation and adsorption conditions on the adsorption performance of the rubidium ion-imprinted polymer were investigated.The results indicated that the rubidium ion-imprinted polymer has high selectivity and faster kinetics than other adsorbents,with an equilibrium adsorption capacity of 200.19 mg·g^(-1)at 298 K within 25 min.The sorption isotherm was well described by the Freundlich isotherm model,while the adsorption kinetics fitted the pseudo-second-order kinetic model.Consecutive adsorption-desorption experiments showed that the ion-imprinted polymer had good chemical stability and reusability.

Adsorption and Adsorption-Photocatalytic Degradation of VOCs Based on Carbon Materials

Adsorption and the combination of adsorption and photocatalysis are prospective strategies for treating lowconcentrationvolatile organic compounds (VOCs). Behind the adsorption technology of VOC treatments are carbon-basedmaterials with large surface areas and high VOC uptake. This review summarizes the research progress in carbon-basedadsorbents and adsorbent-photocatalysts for VOC removal. Firstly, the VOC adsorption performances of various carbonmaterials, including activated carbon, activated carbon fiber, biochar, graphene and its derivatives, and carbon nanotubes,are summarized, and the adsorption mechanism of VOCs on carbon materials is analyzed. Then, the VOC adsorptionphotocatalyticproperties of composites comprised of different carbon materials and photocatalysts are presented. Finally,perspectives on the adsorption and adsorption-photocatalysis of VOCs via carbon materials are proposed. This reviewprovides an optimal reference for the research and development of adsorbents and adsorption-photocatalysts of VOCs.

Mechanochemical synthesis of oxygenated alkynyl carbon materials with excellent Hg(Ⅱ) adsorption performance from CaC2 and carbonates

Adsorptive removal of heavy metal ions from wastewater is very important,and the key is the development of efficient sorbents.In this work,oxygenated alkynyl carbon materials(OACMs)were synthesized via mechanochemical reaction of CaC_(2) and a carbonate(CaCO_(3),Na2CO_(3),or NaHCO_(3))at ambient temperature.The resultant OACMs are micro mesoporous carbon nanomaterials with high specific area(>648 m2 g^(-1)),highly crosslinked texture,and rich alkynyl and oxygenated groups.The OACMs exhibit excellent Hg(Ⅱ)adsorption due to the soft acid-soft base interaction between alkynyl and Hg(Ⅱ),and OACM-3 derived from CaC_(2) and NaHCO_(3) has the saturated Hg(Ⅱ)adsorbance of 483.9 mg g^(-1)along with good selectivity and recyclability.The adsorption is mainly chemisorption following the Langmuir mode.OACM-3 also shows high adsorbance for other heavy metal ions,e.g.256.6 mg g^(-1)for Pb(II),232.4 mg g^(-1)for Zn(II),and 198.7 mg g^(-1)for Cu(II).This work expands the mechnochemical reaction of CaC_(2)with carbonates and possibly other oxyanionic salts,provides a new synthesis approach for functional alkynyl carbon materials with excellent adsorption performance for heavy metal ions,as well as a feasible approach for CO2 resource utilization.

Experimental and Numerical Research on Water Transport during Adsorption and Desorption in Cement-Based Materials

The durability of cement-based materials is related to water transport and storage in their pore network under different humidity conditions.To understand the mechanism and characteristics of water adsorption and desorption processes from the microscopic scale,this study introduces different points of view for the pore space model generation and numerical simulation of water transport by considering the“ink-bottle”effect.On the basis of the pore structure parameters(i.e.,pore size distribution and porosity)of cement paste and mortar with water-binder ratios of 0.3,0.4 and 0.5 obtained via mercury intrusion porosimetry,randomly formed 3D pore space models are generated using two-phase transformation on Gaussian random fields and verified via image analysis method of mathematical morphology.Considering the Kelvin-Laplace equation and the influence of“ink-bottle”pores,two numerical calculation scenarios based on mathematical morphology are proposed and applied to the generated model to simulate the adsorption-desorption process.The simulated adsorption and desorption curves are close to those of the experiment,verifying the effectiveness of the developed model and methods.The obtained results characterize water transport in cement-based materials during the variation of relative humidity and further explain the hysteresis effect due to“ink-bottle”pores from the microscopic scale.

Fabrication of Core-Shell Hydrogel Bead Based on Sodium Alginate and Chitosan for Methylene Blue Adsorption

A novel core-shell hydrogel bead was fabricated for effective removal of methylene blue dye from aqueous solutions.The core,made of sodium alginate-g-polyacrylamide and attapulgite nanofibers,was cross-linked by Calcium ions(Ca^(2+)).The shell,composed of a chitosan/activated carbon mixture,was then coated onto the core.Fourier transform infrared spectroscopy confirmed the grafting polymerization of acrylamide onto sodium alginate.Scanning electron microscopy images showed the core-shell structure.The core exhibited a high water uptake ratio,facilitating the diffusion of methylene blue into the core.During the diffusion process,the methylene blue was first adsorbed by the shell and then further adsorbed by the core.Adsorption tests showed that the coreshell structure had a larger adsorption capacity than the core alone.The shell effectively enhanced the adsorption capacity to methylene blue compared to the single core.Methylene blue was adsorbed by activated carbon and chitosan in the shell,and the residual methylene blue diffused into the core and was further adsorbed.

Adsorption behavior of phosphate on Lanthanum(Ⅲ) doped mesoporous silicates material

A series of lanthanum doped meosoporous MCM-41 （LaxM41, x is Si/La molar ratio） was prepared by sol-gel method. The surface structure of the materials was investigated with X-ray diffraction and N2 adsorption/desorption technique. The content of La in the materials was determined by ICE It was found that the La content of La25M41, La50M41 and La100M41 was 7.53%, 3.89% and 2.32%, respectively. The phosphate adsorption capacities increased with increasing amount of La incorporation. With 0.40 g La25M41 99.7% phosphate could be removed. The effects of Si/La molar ratio, LaxM41 dose, pH, initial concentration of phosphate solution, co-ions on phosphate adsorption were also evaluated. The phosphate adsorption kinetics of LaxM41 could be well-described by the pseudo second-order model, and Langmuir isotherm fit equilibrium data much better than the Freundlich isotherm.

Adsorption of Cu(Ⅱ) on humic acids derived from different organic materials

The adsorption of Cu（Ⅱ） from aqueous solution onto humic acid （HA） which was isolated from cattle manure （CHA）, peat （PHA）, and leaf litter （LHA） as a function of contact time, pH, ion strength, and initial concentration was studied using the batch method. X-ray absorption spectroscopy （XAS） was used to examine the coordination environment of the Cu（ll） adsorbed by HA at a molecular level. Moreover, the chemical compositions of the isolated HA were characterized by elemental analysis and solid-state 13C nuclear magnetic resonance spectroscopy （NMR）. The kinetic data showed that the adsorption equilibrium can be achieved within 8 h. The adsorption kinetics followed the pseudo-second-order equation. The adsorption isotherms could be well fitted by the Langmuir model, and the maximum adsorption capacities of Cu（ll） on CHA, PHA, and LHA were 229.4,210.4, and 197.7 mg g-1, respectively. The adsorption of Cu（Ⅱ） on HA increased with the increase in pH from 2 to 7, and maintained a high level at pH〉7. The adsorption of Cu（Ⅱ） was also strongly influenced by the low ionic strength of 0.01 to 0.2 mol L-1 NaNO3, but was weakly influenced by high ionic strength of 0.4 to 1 mol L-1 NaNO3. The Cu（Ⅱ） adsorption on HA may be mainly attributed to ion exchange and surface complexation. XAS results revealed that the binding site and oxidation state of Cu adsorbed on HA surface did not change at the initial Cu（Ⅱ） concentrations of 15 to 40 mg L 1. For all the Cu（Ⅱ） adsorption samples, each Cu atom was surrounded by 40/N atoms at a bond distance of 1.95 A in the first coordination shell. The presence of the higher Cu coordination shells proved that Cu（Ⅱ） was adsorbed via an inner-sphere covalent bond onto the HA surface. Among the three HA samples, the adsorption capacity and affinity of CHA for Cu（Ⅱ） was the greatest, followed by that of PHA and LHA. All the three HA samples exhibited similar types of elemental and functional groups, but different contents of elemental and functional groups. CHA contained larger proportions of methoxyl C, phenolic C and carbonyl C, and smaller proportions of alkyl C and carbohydrate C than PHA and LHA. The structural differences of the three HA samples are responsible for their distinct adsorption capacity and affinity toward Cu（Ⅱ）. These results are important to achieve better understanding of the behavior of Cu（Ⅱ） in soil and water bodies in the presence of organic materials.

Spongy acetylenic carbon material prepared by ball milling CaC2 and chlorinated rubber—Its mercury adsorption and electrochemical property

Design and preparation of novel advanced carbon materials with unique architecture and functional groups is of great significance.Herein,a spongy acetylenic carbon material(SACM) was prepared through mechanochemical reaction of CaC2 and chlorinated rubber in a planetary ball mill at ambient temperature.Its composition and structure were characterized,and its electrochemical properties and adsorption performance for Hg^2+ were studied.The SACM is composed of submicron spongy aggregates with high carbon content(81.8%) and specific area(503.9 m^2·g^-1),rich porosity and acetylenic groups.The SACM exhibits excellent adsorption for Hg2+with saturated adsorption amount being 157.1 mg·g^-1,which is superior to conventional carbon materials.Further,it exhibits good electrochemical performance with low equivalent series resistance(0.50 Ω),excellent cycling stability and ideal double layer capacitive behavior.This paper provides a novel and universal synthesis method of spongy carbon materials,and better results can be expected through tuning the pore structure,graphitization degree,and heteroatoms of the target carbon materials.

Magnetically responsive porous materials for efficient adsorption and desorption processes

Magnetically responsive porous materials possess unique properties in adsorption processes such as magneticinduced separation and heat generation in alternating magnetic fields, which greatly facilitates recycling procedures, favors long-term operation, and improves desorption rate, making conventional adsorption processes highly efficient. With increasing interest in magnetic adsorbents, great progress has been made in designing and understanding of magnetically responsive porous materials varying from monoliths to nanoscale particles used for adsorption including oil uptake, removal of hazardous substances from water, deep desulfurization of fuels, and CO2 capture in the past few years. Therefore, a review summarizing the advanced strategies of synthesizing these magnetically responsive adsorbents and the utilization of their magnetism in practical applications is highly desired. In this review, we give a comprehensive overview of this emerging field, highlighting the strategies of exquisitely incorporating magnetism to porous materials and subtly exploiting their magnetic responsiveness. Further innovations for fabricating or utilizing magnetic adsorbents are expected to be fueled. The potential opportunities and challenges are also discussed.

Recent Advances on Porous Materials for Synergetic Adsorption and Photocatalysis

Porous photocatalysts are promising materials capable of simultaneously adsorbing and oxidizing/reducing target species,showing great potentials in environmental remediation and energy generation.This review offered a comprehensive overview of the recent progress in design,fabrication,and applications of porous photocatalysts,including carbon-based semiconductors,metal oxides/sulfides,metal–organic frameworks,and adsorbent–photocatalyst hybrids.The fundamental understanding of the structure–performance relationships of porous materials together with the in-depth insights into the synergetic effects between adsorption and photocatalysis was presented.The strategies to further improve the photocatalytic activity of porous photocatalysts were proposed.This review would provide references and outlooks of constructing efficient porous materials for adsorptive and photocatalytic removal of pollutants and energy production.

Hexavalent Chromium Adsorption from Aqueous Solution by Agricultural Waste Materials

Abilities of agricultural waste materials (walnut shell-WS, rice husk-RH, and peanut hull-PH) were tested as adsorbents for the adsorption of Cr(Ⅵ) from aqueous solution. Batch adsorption experiments were carried out to study the adsorption kinetics mechanism of Cr(Ⅵ) effect of adsorbent dosage, pH, contact time, and temperature. The best results are obtained at 15g/L adsorbent concentration, 60min contact time, 298K temperature, and 50mg/L adsorbate initial concentration at pH 2. The adsorption isotherms, using initial concentrations of Cr(Ⅵ) between 10 and 500mg/L for the Cr(Ⅵ) removal, show the maximum metal uptake capacities of adsorbent were 10.48, 6.71, and 8.54mg/g for WS, RH, and PH, respectively. And the adsorption data fitted well to the Langmuir adsorption isotherm for WS, RH, and PH with correlation coefficients of 0.9862, 0.9723, and 0.9714, respectively. Moreover, the FTIR analysis of WS, RH, and PH before and after adsorption of Cr(Ⅵ) suggested that Cr ions were combined to some functional groups of compounds contained in these materials.

Modeling Water Adsorption and Retention of Building Materials From Pore Size Distribution

Water adsorption and capillarity are key phenomena involved during heat and moisture transfer in porous building materials.They account for interaction between solid matrix,liquid water and moist air.They are considered through Water Vapor Adsorption Isotherm(WVAI)and Retention Curve(RC)functions which are constitutive laws characterizing water activity within a porous medium.The objective of this paper is to present a water vapor adsorption and retention models built from multimodal Pore Size Distribution Function(PSDF)and to see how its parameters modify moisture storage for hygroscopic and near saturation ranges.The microstructure of the porous medium is represented statistically by a bundle of tortuous parallel pores through its PSDF.Firstly,the influence of contact angle and temperature on storage properties were investigated.Secondly,a parametric study was performed to see the influence of the PSDF shape on storage properties.Three cases were studied considering the number of modalities,the weight of each modality and the dispersion around mean radius.Finally,as a validation,the proposed model for WVAI were compared to existing model from literature showing a good agreement.This study showed that the proposed models are capable to reproduce various shapes of storage functions.It also highlighted the link between microstructure and adsorption-retention phenomena.

A Sewage Sludge Derived Composite Material for Adsorption of Antibiotics – Kinetics

A novel sewage-sludge derived composite material was developed for the adsorptive removal of organic pollutants from water. In this study a batch adsorption study was carried out to examine the kinetics of antibiotics adsorption by this composite material. A pseudo-second order kinetics model fits the data extremely well, suggesting that chemical adsorption, rather than physical adsorption, is likely the main mechanism of the separation process.

Synthesis of a New Optoelectronic Material Based on Oriented Adsorption of Dyes to Nanoparticles Surface

Synthesis of the optoelectronic storage material with structure for coating by nanosized metal and azo-dye was reported. The characterization of composites was made by using transmission electron microscope （TEM）, ultraviolet-visible spectrometer （UV-Vis） and thermogravity analyzer （TGA）. It is found that, due to the specific structure, in which azo-dye molecules are oriented and adsorbed on the spherical surface of nanosized metal, the absorption maximum of azo-dye methyl orange shift towards shorter wavelength band. The experimental results show that the proposed technique here wouM offer a promising way to synthesize short wavelength optoelectronic storage material by doping of metal nanoparticles coated with dyes in polymer. Furthermore, the composites based on the structure can present excellent thermal properties suitable for the requirements of optical storage. This new type of material is capable of matching semiconductor laser （GaN） in optoelectronic storage technology.

Study on the Adsorption of Preservatives by Eyeliner Pen Packaging Materials

In order to study adsorption of preservatives by eyeliner pen package,the chemical compositions of the commercially available Eyeliner package were analyzed by infrared spectrometer.It was found that these package components were PP,PET,modified PP,modified PET,ABS,nylon,PU and so on.The adsorption effects of these components on three preservatives,i.e.phenoxyethanol,Methyl paraben and Propyl paraben have been further studied by high performance liquid chromatography.The results demonstrated that the four chemical materials PET,PP,modified PP and ABS had no adsorption on the above three preservatives.However,the component named of water diversion core which was composed of modified PET,and nylon-made cotton head have been observed of slight adsorption in this study.And components as the function of preventing liquid leakage,which was made of PU,have presented the most serious adsorption on these three preservatives,with the adsorption order as Propyl Paraben>Methyl Paraben>phenoxyethanol.

Unfolding the structure-property relationships of Li_(2)S anchoring on two-dimensional materials with high-throughput calculations and machine learning

Lithium-sulfur(Li-S)batteries are notable for their high theoretical energy density,but the‘shuttle effect’and the limited conversion kinetics of Li-S species can downgrade their actual performance.An essential strategy is to design anchoring materials(AMs)to appropriately adsorb Li-S species.Herein,we propose a new three-procedure protocol,named InfoAd(Informative Adsorption)to evaluate the anchoring of Li_(2)S on two-dimensional(2D)materials and disclose the underlying importance of material features by combining high-throughput calculation workflow and machine learning(ML).In this paradigm,we calculate the anchoring of Li_(2)S on 12552D A_(x)B_(y)(B in the VIA/VIIA group)materials and pick out 44(un)reported nontoxic 2D binary A_(x)B_(y)AMs,in which the importance of the geometric features on the anchoring effect is revealed by ML for the first time.We develop a new Infograph model for crystals to accurately predict whether a material has a moderate binding with Li_(2)S and extend it to all 2D materials.Our InfoAd protocol elucidates the underlying structure-property relationship of Li_(2)S adsorption on 2D materials and provides a general research framework of adsorption-related materials for catalysis and energy/substance storage.

Materials Studio在金属有机框架材料中气体吸附的应用

综述了全尺度材料模拟软件(materials studio,MS)在MOFs中气体吸附方面的研究进展,重点介绍了MOFs中气体吸附模拟计算时MS软件各个模块的应用。对采用MS软件模拟计算MOFs中气体吸附性能提出了一些建议。

Measurement of Atrazine Adsorption onto Surficial Sediments(Natural Surface Coatings)——New Evidence for the Importance of Fe Oxides

To reveal the relative contribution of the components, Fe, Mn oxides or organic materials（OMs） in the surficial sediments（SSs）, and the natural surface coating samples（NSCSs） to adsorbing atrazine（AT）, a selective chemical extraction technique was employed, to remove the different components, and the adsorption characteristics of AT on the SSs and the NSCSs were investigated. The observed adsorptions of AT on the original and extracted SSs and NSCSs were analyzed by nonlinear least squares fitting（NLSF） to estimate the relative contribution of the components. The results showed that the maximum adsorption of AT on the NSCSs was greater than that in the SSs, before and after extraction treatments, implying that the NSCSs were more dominant than the SSs for organic pollutant adsorption. It was also found that the Fe oxides, OMs, and residues in SSs（NSCSs） facilitated the adsorption of AT, but Mn oxides directly or indirectly restrained the interaction of AT with SSs（NSCSs） particles. The contribution of the Fe oxides to AT adsorption was more than that of OMs; the greatest contribution to AT adsorption on a molar basis was from the Fe oxides in the nonresidual fractions, indicating that the Fe oxides played an important role in controlling the environmental behavior of AT in an aquatic environment.